A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6729



Internal ID15551667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129789659..129814916hg38UCSC Ensembl
Outerchr9:132551938..132577195hg19UCSC Ensembl
Outerchr9:131591759..131617016hg18UCSC Ensembl
Outerchr9:129631492..129656749hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386648
hg196648
hg186648
hg176648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8671
SamplesNA12156
Known GenesTOR1A, TOR1B
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6729
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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